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Active, not recruitingNCT07808840Updated Sep 9, 2026

Using Wet Towel During Labor

An interventional study of Wet Towel in Labor Pain, Comfort and Labor Anxiety, sponsored by Sakarya University. Active, not recruiting at 1 site in Turkey (Türkiye). Open to female participants aged 18 Years to 45 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-09-09.

Sponsored by Sakarya University · Not applicable, Interventional, and Supportive care

Phase
Not applicable
Study type
Interventional
Enrollment
60
Allocation
Randomized
Ages
18 Years to 45 Years
Sex
Female
01

Study summary

The goal of this clinical trial is to learn whether the wet towel method applied during the first stage of labor can reduce labor pain and anxiety and improve childbirth comfort in first-time mothers. The main questions it aims to answer are:

Does the wet towel method reduce labor pain? Does the wet towel method improve childbirth comfort? Does the wet towel method reduce anxiety during labor?

Researchers will compare women who receive the wet towel method in addition to routine intrapartum care with women who receive routine intrapartum care alone to determine whether the intervention improves maternal outcomes during labor.

Participants will:

Be randomly assigned to either the wet towel intervention group or the routine care control group.

Receive the wet towel application for at least 10 minutes during the active phase of the first stage of labor or receive routine intrapartum care only.

Complete assessments of labor pain, childbirth comfort, and anxiety before and after the intervention using validated measurement tools

Read the detailed description

This randomized controlled trial aims to evaluate the effects of the wet towel method applied during the first stage of labor on labor pain, childbirth comfort, and anxiety levels among primiparous women. Labor pain and anxiety may negatively affect the childbirth experience, prolong labor, and reduce maternal comfort. Although several non-pharmacological methods have been shown to improve maternal outcomes during labor, evidence regarding the effectiveness of the wet towel method remains limited.

The study will be conducted at the Labor and Delivery Unit of Sakarya Training and Research Hospital. Sixty low-risk primiparous pregnant women will be randomly assigned to either an intervention group (wet towel application) or a control group receiving routine intrapartum care. In the intervention group, a clean towel will be placed over the woman's head and shoulders, and warm water (36-38°C) will be gently applied over the towel for at least 10 minutes during the active phase of labor. Participants in both groups will be assessed before and after the intervention.

Primary outcomes include labor pain, childbirth comfort, and anxiety during labor. Pain will be assessed using the Visual Analog Scale (VAS), comfort using the Childbirth Comfort Questionnaire, and anxiety using the Anxiety Assessment Scale for Pregnant Women in Labor. The findings of this study are expected to provide evidence regarding the effectiveness of the wet towel method as a simple, safe, low-cost, and non-pharmacological intervention to improve maternal comfort and reduce pain and anxiety during labor.

02

Conditions studied

  • Labor Pain
  • Comfort
  • Labor Anxiety

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Keywords

  • Labor
  • Wet Towel Method
  • Vaginal Birth
  • Randomized Controlled Trial
03

In context

Labor Pain

423 studies on the registry are indexed under Labor Pain; 74 are open to participants now.

This study's planned enrollment of 60 is below the median of 100 across 347 interventional studies indexed under Labor Pain.

Browse Labor Pain studies →

Lead sponsor

Sakarya University is the lead sponsor of 190 studies on the registry; 53 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 45 Years
Sexes eligible
Female
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Pregnant women admitted to the delivery room for childbirth
  • Pregnant women without any risks
  • Pregnant women with sufficient language proficiency to communicate effectively
  • Women experiencing their first pregnancy

Exclusion criteria

Exclusion Criteria:

  • Pregnant women admitted for a planned cesarean section
  • Pregnant women who do not agree to participate in the study
05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
60 participants (estimated)

Study arms

  • Experimental
    wet Towel group

    Other: Wet Towel

  • No intervention
    control

Interventions

  • OtherWet Towel

    A woman who has entered the active phase and is being treated will be safely escorted to the bathroom and prepared for the procedure. A clean towel will be placed over the woman's head and shoulders, and water at an appropriate temperature (approximately 36-38°C) will be directed in a slow stream from the showerhead onto the towel. The water flow will be adjusted so that it gently touches the head area through the towel, and the procedure will be continued for at least 10 minutes. During this process, the woman will be continuously monitored, her comfort and safety will be ensured, and the fetal heart rate will be monitored in accordance with institutional protocol. After the procedure is completed, the woman's head and shoulders will be dried, and she will be taken back to her room for further assessment. Translated with DeepL.com (free version)

06

What researchers measure

Primary outcomes

  1. Pain intensity assessed by Visual Analog Scale (VAS)

    The primary outcome of this study is to evaluate the effect of wet towel application on labor pain intensity. Pain intensity will be assessed using the Visual Analog Scale (VAS) before and after the intervention.The primary outcome is labor pain intensity, assessed using the Visual Analog Scale before and after the intervention. Scores range from 0 to 10, with higher scores indicating greater labor pain intensity.

    Time frame: Before intervention and immediately after intervention during the active phase of labor.

  2. Childbirth comfort level assessed by Childbirth Comfort Questionnaire

    The effect of wet towel application on childbirth comfort levels will be evaluated using the Childbirth Comfort Questionnaire before and after the intervention. Total scores range from 9 to 45, with higher scores indicating a higher level of childbirth comfort.

    Time frame: Before intervention and immediately after intervention.

  3. Anxiety level during labor assessed by Anxiety Assessment Scale for Pregnant Women in Labor

    The effect of wet towel application on anxiety levels during labor will be evaluated. Anxiety level during labor will be assessed using the Scale for Assessing the Anxiety Status of Pregnant Women in Labor before and after the intervention. The mean score ranges from 1 to 5, with higher scores indicating higher levels of anxiety during labor.

    Time frame: Before intervention and immediately after intervention.

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Study locations

1 site
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References and documents

Publications

  • Shishido I, Konya I, Yano R. Effect on autonomic nervous activity of applying hot towels for 10 s to the back during bed baths. J Physiol Anthropol. 2020 Nov 19;39(1):35. doi: 10.1186/s40101-020-00245-7. PubMed 33213514 ↗
  • Mellado-Garcia E, Diaz-Rodriguez L, Cortes-Martin J, Sanchez-Garcia JC, Piqueras-Sola B, Macias JCH, Rivas Ruiz F, Rodriguez-Blanque R. Comparative Analysis of Therapeutic Showers and Bathtubs for Pain Management and Labor Outcomes-A Retrospective Cohort Study. J Clin Med. 2024 Jun 15;13(12):3517. doi: 10.3390/jcm13123517. PubMed 38930046 ↗
  • Taskin A, Ergin A. Effect of hot shower application on pain anxiety and comfort in the first stage of labor: A randomized controlled study. Health Care Women Int. 2022 May;43(5):431-447. doi: 10.1080/07399332.2021.1925282. Epub 2021 Jun 22. PubMed 34156915 ↗

Individual participant data

Plan to share: No — Individual participant data will not be shared because the data contain sensitive health information from pregnant women. To protect participant confidentiality and privacy, only aggregated results will be reported.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 9, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07808840
Lead sponsor
Sakarya University
Responsible party
Yasemin Hamlaci Baskaya (Associate Professor, Principal Investigator, Sakarya University) — Principal investigator
First posted
Sep 9, 2026
Start date
Aug 25, 2026
Primary completion
Nov 30, 2026 (estimated)
Completion
Dec 30, 2026 (estimated)
Last update
Sep 9, 2026

Study contacts

YASEMİN BAŞKAYA
study director · Sakarya University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in Sep 2026. You cannot join it, but the record below documents what was studied.

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